Recent advances in tau-directed immunotherapy against Alzheimer’s disease: an overview of pre-clinical and clinical development

被引:0
作者
Pei Ying Ng
I Shuen Chang
Rhun Yian Koh
Soi Moi Chye
机构
[1] International Medical University,School of Postgraduate
[2] International Medical University,School of Health Science, Division of Biomedical Science and Biotechnology
来源
Metabolic Brain Disease | 2020年 / 35卷
关键词
Alzheimer’s disease; Tubulin-associated unit; Tauopathy; Immunotherapy; Active immunisation; Passive immunisation;
D O I
暂无
中图分类号
学科分类号
摘要
Alzheimer’s disease (AD) has been a worldwide concern for many years now. This is due to the fact that AD is an irreversible and progressive neurodegenerative disease that affects quality of life. Failure of some Phase II/III clinical trials in AD targeting accumulation of β-amyloid in the brain has led to an increase in interest in studying alternative treatments against tubulin-associated unit (Tau) pathology. These alternative treatments include active and passive immunisation. Based on numerous studies, Tau is reported as a potential immunotherapeutic target for tauopathy-related diseases including AD. Accumulation and aggregation of hyperphosphorylated Tau as neuropil threads and neurofibrillary tangles (NFT) are pathological hallmarks of AD. Both active and passive immunisation targeting Tau protein have shown the capabilities to decrease or prevent Tau pathology and improve either motor or cognitive impairment in various animal models. In this review, we summarise recent advances in active and passive immunisation targeting pathological Tau protein, and will discuss with data obtained from both animal and human trials. Together, we give a brief overview about problems being encountered in these immunotherapies.
引用
收藏
页码:1049 / 1066
页数:17
相关论文
共 828 条
[1]  
Agadjanyan MG(2017)Humanized monoclonal antibody armanezumab specific to N-terminus of pathological tau: characterization and therapeutic potency Mol Neurodegener 12 33-6928
[2]  
Zagorski K(2001)Hyperphosphorylation induces self-assembly of into tangles of paired helical filaments/straight filaments Proc Natl Acad Sci 98 6923-593
[3]  
Petrushina I(2017)Preclinical characterization of an antibody [LY3303560] targeting aggregated tau Alzheimers Dement 13 592-1750
[4]  
Davtyan H(2019)Prevention of tau seeding and propagation by immunotherapy with a central tau epitope antibody Brain 142 1736-5454
[5]  
Kazarian K(2005)Cell-cycle reentry and cell death in transgenic mice expressing nonmutant human tau isoforms J Neurosci 25 5446-9129
[6]  
Antonenko M(2007)Immunotherapy targeting pathological tau conformers in a tangle mouse model reduces brain pathology with associated functional improvements J Neurosci 27 9115-17507
[7]  
Davis J(2013)Activation of asparaginyl endopeptidase leads to tau hyperphosphorylation in Alzheimer disease J Biol Chem 288 17495-1378
[8]  
Bon C(2011)Tau-targeted immunization impedes progression of neurofibrillary histopathology in aged P301L tau transgenic mice PLoS One 6 1371-485
[9]  
Blurton-Jones M(1985)The distribution of tau in the mammalian central nervous system J Cell Biol 101 472-11666
[10]  
CRibbs DH(2010)Efficacy and safety of immunization with phosphorylated tau against neurofibrillary tangles in mice Exp Neurol 24 16559-667